Study On Regulatory Of Drug In China

Drug is a kind of substance which can defend, therapy and diagnose disease for human been. It also can accommodate physical enginery purposely. It is a kind of special commodity and has indications, direction and dosage. Drug regulatory is surveillance and administer in macro-category. Government carries it out by establishing and promulgating rule of law and standard fiercely. In order to insure drug security, effectiveness and economy, the regulatory of drug pays it attention to the surveillance of drug development, manufacture, supply and use. Since 20 century, drug administration has been accredit by legislation and exerts surveillance function. SFDA and other department have promulgated a series of rules and law and the relative policy to insure drug security for people. But there are still some problems in drug administration and they show two things for us. One is that the drug manufactures and suppliers have careless omission in guarantee of drug security, the other is that some thing to be perfect in drug administration and we have to do our best to conquer them. So this text gives some strategies according to the study on the other countries and our factual situation in drug administration.The text studies the relative concepts and the theory of surveillance and organization firstly and then analyses EU, USA's drug administration and get some useful inspire. The text finds out the problems through analyzing the surveillance of drug. On the foundation of the above study, the text gives the policies to advance the effect of surveillance. These policies include two aspects: one is the surveillance of administration: set up job description and personal appraisement, change the regulatory manner; the other is strengthening the support from others: how to make guild to exert its function and change the information dissymmetry.